Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152 0.821 0.214 None NA snp 0.41 15
rs687289 0.923 0.143 None NA snp 0.39 9
rs13389219 1.000 0.071 2 164672366 C/T snp 0.46 4
rs507666 0.846 0.036 None NA snp 0.17 4
rs10107366 8 98101459 T/C snp 1.7E-02 1
rs11696845 20 44742679 C/T snp 0.33 1
rs641862 13 110137885 T/C snp 1.4E-02 1
rs7012789 8 126904963 A/G,T snp 0.45 1
rs8037818 15 32635275 C/T snp 0.78 1
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 16
rs2074356 0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03 11
rs8050136
FTO
0.744 0.321 16 53782363 intron variant C/A snp 0.40 10
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 10
rs1121980
FTO
0.923 0.107 16 53775335 intron variant G/A,C snp 0.44 8
rs9940128
FTO
0.923 0.071 16 53766842 intron variant G/A snp 0.42 6
rs9930506
FTO
1.000 0.071 16 53796553 intron variant A/G snp 0.36 5
rs10830963 0.846 0.179 11 92975544 intron variant C/G snp 0.24 4
rs7193144
FTO
0.923 0.107 16 53776774 intron variant T/C snp 0.40 4
rs10195252 1.000 0.071 2 164656581 intron variant T/C snp 0.47 3
rs3741298 11 116786845 intron variant C/T snp 0.74 3
rs6795735 0.923 0.107 3 64719689 intron variant C/A,G,T snp 0.54 3
rs863002 1 159205130 intron variant C/T snp 0.29 3
rs9939973
FTO
1.000 0.071 16 53766656 intron variant G/A snp 0.42 3
rs10747502 1.000 0.036 1 99058491 intron variant A/G snp 0.86 2
rs11231693 11 64095140 intron variant G/A snp 0.12 2